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作 者:王迎昕[1] 张小燕[2] 张宝峰[2] 张可浩[2] 方静[2] 胡莺[2] 翟宁[2] 陈锡美[1] 郜恒骏[1]
机构地区:[1]上海同济大学附属同济医院消化疾病研究所,200065 [2]生物芯片上海国家工程研究中心
出 处:《中华消化杂志》2009年第2期114-117,共4页Chinese Journal of Digestion
基 金:上海市启明星科研计划资助项目(07QB14037)
摘 要:目的探讨无淋巴结转移结肠癌微小核糖核酸(microRNA)表达谱,筛选与结肠癌早期发生、发展相关的特异性microRNA。方法选取手术、病理证实未发生淋巴结转移的结肠癌及大于癌旁5cm结肠组织标本各3例,抽提分离miRNA,与Agilent microRNA基因芯片杂交,并进行图像和数据分析。运用microRNA特异引物对差异表达的microRNA进行荧光定量实时聚合酶链反应(RT—PCR)验证。结果筛选出在结肠癌中差异表达的microRNA有14个,其中12个microRNA表达水平增高,分别为miR-106b、miR-135b、miR-18a、miR-18b、miR-196b、miR-19a、miR-224、miR-335、miR-424、miR-20a^*、miR-301b和miR-374a;2个microRNA表达水平降低,分别为miR-378和miR-378^*。miR-106b和miR-19a下游存在符合要求的靶基因数目众多。检测了芯片中显示表达上调的miR-18a和miR135b在3例结肠癌组织和癌旁组织中的表达,结果显示miR-18a和miR135b在3例癌组织和癌旁组织中表达均上调;荧光定量RT-PCR结果与microRNA芯片的结果符合。结论miR-106b、miR-135b、miR-18a、miR-18b、miR-196b等microRNA在结肠癌与癌旁组织中存在差异表达,预测其下游靶基因中大部分与肿瘤相关,提示它们可能在结肠癌早期发生、发展过程中起着重要的调控作用。Objective To investigate microRNA expression profiles of colonic cancer without lymph node metastasis and identify the specific microRNAs associated with carcinogenesis of colon. Methods Cancerous and para-cancerous tissues (5 cm from cancer tissues of the colon) confirmed without lymph node metastasis were collected from 3 patients. The microRNAs were extracted and isolated by mirVana RNA kit. Hybridizations were made by applying the microRNAs to Agilent microRNA mieroarray. Data analysis was done by software of Feacture Extraction. The discovered microRNAs were confirmed by real time PCR assay. Results Twelve out of 14 microRNAs associated with colonic cancer were up-regulated in colonic tissues. They were miR 106b, miR 135b, miR-18a, miR-18b,miR-196b, miR-19a, miR-224, miR-335, miR-424, miR-20a^*, miR-301b and miR 374a. The rest two of miR-378 and miR-378^* were down-regulated. Two up-regulated microRNAs (miR 18a and miR-135b) were detected in 3 pairs of cancerous and para-cancerous tissues. The expression level of miR-18a and miR-135b were accordant with the results of real time PCR. Conclusions microRNA, such as miR-106b,miR-135b,miR-18a,miR-18b,miR-196b, ect, were differentially expressed between cancerous and para-cancerous tissues. Many of these target genes are supposed to participate in the process of multiple tunmorgenesis. These microRNAs play an important role in the carcinogenesis of colon.
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